A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485727



Internal ID21143280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61778131..61804245hg38UCSC Ensembl
chr14:62244849..62270963hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3826115
hg1926115
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189491
Samples
Known GenesSNAPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485727
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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